About this Journal Submit a Manuscript Table of Contents
International Journal of Microbiology
Volume 2012 (2012), Article ID 358305, 8 pages
http://dx.doi.org/10.1155/2012/358305
Review Article

Dermatophyte Virulence Factors: Identifying and Analyzing Genes That May Contribute to Chronic or Acute Skin Infections

1Seattle Biomedical Research Institute, 307 Westlake Avenue North, Suite 500, Seattle, WA 98109-5219, USA
2School of Biological Sciences, University of Missouri-Kansas City, 5007 Rockhill Road, BSB 404, Kansas City, MO 64110, USA

Received 14 July 2011; Accepted 9 August 2011

Academic Editor: Julian R. Naglik

Copyright © 2012 Rebecca Rashid Achterman and Theodore C. White. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Dermatophytes are prevalent causes of cutaneous mycoses and, unlike many other fungal pathogens, are able to cause disease in immunocompetent individuals. They infect keratinized tissue such as skin, hair, and nails, resulting in tinea infections, including ringworm. Little is known about the molecular mechanisms that underlie the ability of these organisms to establish and maintain infection. The recent availability of genome sequence information and improved genetic manipulation have enabled researchers to begin to identify and study the role of virulence factors of dermatophytes. This paper will summarize our current understanding of dermatophyte virulence factors and discuss future directions for identifying and testing virulence factors.

1. Introduction

Dermatophytes are the most common cause of fungal infections worldwide, resulting in treatment costs of close to half a billion dollars annually in the USA [1, 2]. The World Health Organization estimates global prevalence of dermatomycoses to be approaching 20% [3]. Despite this, researchers lack a sophisticated understanding of dermatophyte pathogenesis [4].

Dermatophytes are the group of filamentous fungi that are the most common cause of cutaneous mycoses. The diseases caused by these organisms are generally named after the part of the body that is infected rather than the infecting organism. For example, tinea pedis refers to athlete’s foot and tinea unguium refers to a nail infection. Dermatophyte infections are generally superficial, but immunocompromised patients can experience severe, disseminated disease [5]. Although dermatophyte infections are treatable, there is a high rate of reinfection; it remains to be determined whether this is due to relapse (the fungus not being completely eradicated during treatment) or a new infection [6].

The dermatophytes include three genera of molds in the class Euascomycetes: Trichophyton, Microsporum, and Epidermophyton. Dermatophytes are grouped according to their habitat as being either anthropophilic (human associated), zoophilic (animal associated), or geophilic (soil dwelling). Anthropophilic species are responsible for the majority of human infections; however, species from all three groups of dermatophytes have been associated with clinical disease. Human infections caused by anthropophiles tend to be chronic, with little inflammation, whereas infections caused by geophiles and zoophiles are often associated with acute inflammation and are self-healing [7].

The recent sequencing and annotation of several dermatophyte genomes, as well as advances in techniques for genetic manipulation of dermatophytes, provide resources that will aid in elucidating the mechanisms of virulence of these ubiquitous organisms. An understanding of the specific virulence factors that contribute to dermatophyte pathogenesis would aid in the design of effective therapeutics. This paper will summarize the current state of understanding of dermatophyte virulence factors and comment on future directions for their studies.

2. Virulence Factor Identification

2.1. Virulence Factor Identification Using Bioinformatics Approaches

The sequencing of seven dermatophyte genomes has recently been completed, and the sequences have been made publically available via the Broad Institute database [8]. The Broad Institute sequenced and annotated the genomes of five dermatophyte species. Trichophyton rubrum (Tr) is anthropophilic and the most common cause of dermatophyte infections in humans worldwide. Trichophyton tonsurans (Tt) is also anthropophilic and is a major cause of tinea capitis (scalp ringworm). Tt was recently found to be present in more than 30% of students in some grade levels at US schools [9]. Trichophyton equinum (Te) is closely related to Tt but is zoophilic and primarily associated with disease in horses. Microsporum canis (Mc) is also zoophilic and is the most common cause of tinea capitis in Europe [10]. Microsporum gypseum (Mg) is a geophile that is associated with gardener’s ringworm. The strains selected for sequencing are all clinically relevant (associated with human disease) [4] and have been characterized with respect to growth rate, conidiation, and drug susceptibility [11]. Genome sequences of the remaining two species, the phylogenetically related zoophiles Arthroderma benhamiae (Ab, a teleomorph of Trichophyton mentagrophytes) and Trichophyton verrucosum (Tv), were recently completed by the Hans Knoell Institute (Jena, Germany) and published [12]. These organisms cause a highly inflammatory infection in humans. As expected, comparison of the seven dermatophyte genomes indicates that these species are closely related phylogenetically and each is more closely related to the others than to Coccidioides immitis or the dimorphic fungi (unpublished data). This is in agreement with a comparative study of five dermatophyte mitochondrial genomes, which suggested a recent divergence of the dermatophyte clade [13].

All seven genomes were found to encode high numbers of protease-encoding genes compared to related, nondermatophytic fungi ([12] and unpublished data). In particular, dermatophytes appear to have expanded sets of endopeptidases, exopeptidases, and secreted proteases. In contrast, there is little difference in abundance of carbohydrate enzymes of the CAZy family designation [14, 15] between dermatophytes and dimorphic fungi (unpublished data). This highlights the important role of protein degradation in the lifestyle of dermatophytes.

Secretome analysis of Ab during growth on keratin confirmed that proteases made up the largest group of identified secreted proteins [12]. The Ab and Tv genome sequences also revealed a relatively high number of secondary metabolite gene clusters, and expression of some of these genes were confirmed to be up- or downregulated during keratinocyte infection by Ab [12].

As described above, disease caused by human-adapted organisms Tr and Tt tends to be chronic with low inflammation, whereas zoophiles (Te, Mc, Ab) and geophiles (Mg) generally cause an inflammatory infection. The availability of sequence information now allows researchers to use a bioinformatics approach to make predictions about which genes are involved in virulence, as well as differences between species that have adapted to different ecological niches. Preliminary unpublished analysis indicates that among the five genomes sequenced by the Broad Institute, most genes are conserved in all five species, the majority of which are annotated. This is not surprising and confirms the genetic relatedness of the dermatophytes. Of the annotated genes that are unique to a particular species, there does not appear to be any trend. However, there are a number of hypothetical genes unique to each species that potentially play a role in niche adaptation and pathogenicity (unpublished data).

In many pathogenic eukaryotes, including protozoan parasites and fungi, there is a trend for clinical isolates to have cryptic, modified sexual cycles. Although originally thought to be asexual, Aspergillus fumigatus, Candida albicans, and Cryptococcus neoformans are all examples of fungi that cause systemic disease and were shown to have sexual cycles [16, 17]. It is therefore possible that other pathogenic fungi, including anthropophilic dermatophytes, have sexual cycles that have not yet been identified under laboratory conditions. Bioinformatic analysis identified the mating locus in each of the sequenced dermatophyte species, and PCR analysis with additional strains of the species has identified the other mating type, except for Tr, where the second mating type has not yet been identified [18]. Recent work has shown normal mating with progeny in the geophilic species Mg [19] and the ability of Tr to initiate but not complete a mating cycle with a related species of the opposite mating type [20]. Whether Tr is able to mate during growth on human skin remains to be determined, and the potential contributions of mating to virulence represent an area of active research.

Knowledge of the mechanisms of pathogenesis of other fungi also leads to predictions of virulence factors in dermatophytes. For example, the dipeptidyl peptidase DppIV was identified in Mc based on sequence similarity [21]. Additionally, dermatophytes have recently been shown to produce melanin or melanin-like compounds, which are predicted to play a role in virulence based on the known role of melanins in other pathogenic fungi [22]. Similarly, Tr has been shown to produce xanthomegnin, a toxin previously known to be produced by Aspergillus, in culture and during human infection [23]. The complete annotated sequences of dermatophyte genomes will aid in identifying additional putative virulence factors based on sequence similarity, which will then need to be tested experimentally to confirm expression and role during infection.

2.2. Virulence Factor Identification Using High-Throughput Screens

The T. rubrum Expression Database [24, 25] provided an important starting point for transcriptional analysis by collating expressed sequence tags (ESTs) and transcriptional profiles from microarrays, resulting in the identification of numerous genes involved in growth during a variety of conditions. Complete genome sequencing will enhance our ability to identify open reading frames (ORFs) in future studies.

Screens have historically been used to identify gene products likely to play a role in virulence. Dermatophytes are known to infect keratinized structures such as skin, hair, and nails, and therefore the ability of dermatophytes to degrade keratin is considered a major virulence attribute. In support of this, a correlation between keratinase activity and pathogenesis has been observed for Mc [26] and dermatophytes have been shown to secrete more than 20 proteases in vitro when grown in medium containing protein as the sole nitrogen source (reviewed in [27]). As discussed above, genome analysis confirmed expansion of protease genes in the seven dermatophyte genomes ([12] and unpublished data).

Given the importance of keratin to the pathogenic lifestyle of dermatophytes, studies that aimed to identify virulence factors have often examined the response of dermatophytes to growth on keratin. For example, subtractive suppression hybridization (SSH) approaches have been used to compare Tr during growth on keratin as compared to glucose [28] or minimal medium [29]. Select genes identified in this manner were confirmed to be upregulated during interaction with keratinocytes [29]. These included a homeobox transcription factor and a zinc-finger protein, which are candidates for acting as transcriptional regulators during infection.

Kaufman et al. found that thioredoxin, cellobiohydrolase, and the protease-encoding gene Tri m 4 had increased transcription during growth of T. mentagrophytes (Tm) with keratin as compared to glucose alone [30]. Zaugg et al. constructed a cDNA microarray for Tr and examined gene expression during growth on soy and soy + keratin as compared to rich medium (Sabouraud) to find factors induced by one or both proteins [31]. They found that growth in soy or soy + keratin activated a large set of genes encoding secreted endo- and exoproteases, as well as other proteins potentially implicated in protein degradation, some of which appeared to be keratin specific. Interestingly, the authors noted that upregulation of enzymes in the glyoxylate cycle was also observed during growth on soy or soy + keratin, as compared to Sabouraud. The glyoxylate cycle has been implicated in virulence of other microorganisms [32], and its upregulation during dermatophyte growth on keratin was confirmed for Ab by Staib et al., who examined gene expression of Ab under the same conditions [33]. They found induction of similar sets of orthologous protease-encoding genes as compared to the Tr data.

However, a growing body of evidence suggests that not all keratin-induced proteases play a role during infection. For example, although Tri m 4 was induced by the presence of keratin, it was not significantly upregulated when homogenized skin was provided as the sole nutrient source [30]. Furthermore, some of the prominent keratin-induced genes of Ab were not found to be strongly upregulated in vivo during guinea pig infection and the protease-encoding gene SUB6 was strongly upregulated in vivo but not detectably activated during growth on keratin [33]. Instead, Staib et al. found just one protease-encoding gene, MCPA, which was strongly induced during both infection and growth on keratin [33]. Their study identified nonprotease genes, such as those encoding a putative opsin-related protein and enzymes of the glyoxylate cycle, which were upregulated in vivo. Likewise, Burmester et al. found that only some of the keratin-induced proteases were strongly expressed during fungus-keratinocyte interaction [12]. Interestingly, they found that secondary metabolites were induced during interaction with keratinocytes. Previous work has shown that antibiotic substances are produced by dermatophytes that may help the fungi compete against bacteria also present on the skin [34, 35]. It is possible that differentially regulated secondary metabolites, perhaps including antibiotics or pigment production, play a role in dermatophyte infection by providing the fungi with an advantage over other microorganisms present on the skin.

Expression of specific secreted subtilisins and metalloproteases was monitored by RT-PCR during Tr growth in vitro in the presence of keratin, elastin, collagen, or human skin sections [36]. SUB3, SUB4, and MEP4 had increased expression under all four conditions (compared to growth in glucose medium). The increased expression of SUB3 is consistent with in vivo findings in Ab, although SUB3 of Ab was upregulated only at a low level [12]. Furthermore, SUB4 was not found to be upregulated during guinea pig infection by Ab.

Together, these results indicate that secreted proteases are not the only virulence factors of dermatophytes and indeed that not all proteases play an overlapping role during infection. Some proteases may be used only during specific stages of infection or might have a more general role in growth that is not specific to virulence. Furthermore, it is possible that each of the dermatophyte species will have a unique program of expression for proteases and other putative virulence factors during infection.

In order to identify additional factors that play a role during infection, investigators have examined the transcriptional response of dermatophytes exposed to environmental factors such as growth on lipids [37, 38], changes in pH [38, 39], and the presence of antifungal drugs [38, 4045]. They have also assessed transcript abundance during different stages of growth [4649]. The relationship of these environmental factors to the pathogenesis of dermatophytes is a continuing area of research.

3. Testing the Role of Putative Virulence Factors

3.1. Models for Testing Virulence

Although dermatophytes were initially studied in experimental human infections [50], the current most common animal model for studying virulence factors of dermatophytes is the guinea pig [51]. This model has been useful for zoophiles [33, 5254] but does not provide an accurate infection model for most anthropophilic species [4]. A murine model has been useful for studying the immune response to dermatophytes [55, 56], but again the mice only develop disease in response to infection by zoophiles. An alternative to mammalian models has been to rely on growth of the dermatophyte on keratinized surfaces such as sterilized nail fragments as an indication of pathogenicity [57, 58]. Despite its relative ease, this is a nonquantitative model based solely on the observed (qualitative) ability of the dermatophyte to grow. Its continued use in virulence studies highlights the need for development of a more appropriate model of anthropophilic dermatophyte infection.

Galleria mellonella (wax moth) larvae are an established virulence model for several fungal pathogens, including Candida, Cryptococcus, and the mold Aspergillus [5965]. The Galleria model has several advantages as a virulence model, including an immune system with some similarities to the human innate immune system [61, 66]. However, Galleria does not appear to be a useful model to study the pathogenic mechanisms of dermatophytes [11].

Recently, researchers have used skin explants as a model for dermatophyte adherence and invasion [6771]. Tm and Tr have been tested in this model. Conidial suspensions or pieces of mycelium are applied to a skin explant, and germination and hyphal invasion are monitored microscopically. Dermatophytes can adhere to and invade ex vivo skin explants [6769], and dermatophyte growth is inhibited by antifungal drugs [70]. A reconstructed feline epidermal model [72] and a feline ex vivo epidermal model [52] have also been reported for the study of Mc, a zoophile whose natural host is cats.

Human epidermal tissues are commercially available, which abrogates the need for researchers to have access to clinical samples and provides a greater degree of standardization between labs that wish to use skin explants as a virulence model. Dermatophyte microconidia are able to germinate and cause damage to these tissues (our own unpublished data). Skin explants therefore represent a possible virulence model to study the initial stages of dermatophyte infection.

3.2. Virulence Factor Genes That Have Been Tested

There are a few cases in which a gene hypothesized to play a role in virulence has been deleted or knocked down. Due to the historical difficulties of genetic manipulation of dermatophytes, gene deletions are often not complemented. However, recent genetic advances have provided a foundation for genetic manipulation of dermatophytes [53, 7377]. Ideally, future studies of dermatophytes should include both a deletion and a complementation of the mutation to definitively prove the role of a gene product in virulence.

A study on the gene encoding malate synthase (AcuE, a key enzyme of the glyoxylate cycle) provided an excellent step towards this goal. ACUE was identified as being upregulated during infection of guinea pigs by Ab [33]. Grumbt et al. constructed a deletion, acuE, and compared its growth to the parental strain on different carbon sources as well as during guinea pig infection [53]. Although they did not see a difference in pathogenicity between the mutant and the wild type, they did see differences in growth when provided with 0.5% olive oil as the sole carbon source, with acuE being unable to grow. Complementation with the wild-type allele restored growth.

TruMDR2 is a gene identified in Tr that is predicted by sequence similarity to encode an ATP-binding cassette (ABC) transporter protein [78]. Deletion of this gene results in increased susceptibility to some antifungal compounds [78]. TruMDR2 was found to be upregulated during growth in the presence of keratin as compared to glucose [28, 58], suggesting a role for the transporter protein during infection. To confirm this, the wild-type and deletion mutants were compared for growth on nail fragments. As predicted, the deletion mutant showed a reduced ability to grow [58].

Tr also encodes a protein with sequence similarity to pacC, a pH-regulated transcription factor in Aspergillus nidulans [57]. Disruption of pacC results in reduction of keratinolytic activity and a reduction in the ability to grow on nail fragments [57].

As discussed above, SUB3 has been identified in screens as a putative virulence factor in Tr and Ab. SUB3 expression and activity has also been monitored in Mc, where SUB3 was identified as a 31.5 kDa secreted protein with in vitro keratinolytic activity [79]. It was found to be expressed during natural Mc infection of cats, although presence of SUB3 did not correlate to disease state as SUB3 was found in both symptomatic and asymptomatic infections [79, 80]. Expression of SUB3 was experimentally reduced using RNA-mediated silencing [21], and the resulting strain was tested in a feline ex vivo adherence model [52]. Arthroconidia from the SUB3 RNA-silenced M. canis strain had reduced adherence to feline epidermis compared to the control strain. Although the control-strain arthroconidia did not adhere equally well to epidermis from each of three different cats, for each cat the SUB3 RNA-silenced strain had a reduction in adherence that was statistically significant. The strains were also tested for their ability to cause lesions in the guinea pig model, but no difference in virulence was observed [52]. The authors conclude that SUB3 is required for adherence to, but not invasion of, the epidermis. It is also possible that the function of other secreted subtilisins masked the loss of SUB3 or that the guinea pig model does not completely mimic feline infection.

In Mc, the dnr1 gene, which has sequence similarity to nitrogen regulatory genes of other filamentous fungi, is able to complement a loss-of-function nitrogen regulatory mutation (areA) in Aspergillus nidulans. Disruption of dnr1 in Mc caused a reduction in the ability of the fungus to grow on medium containing keratin as the sole nitrogen source [81]. A similar result was seen for Tm (teleomorph: A. vanbreuseghemii) when tnr1, a gene with sequence similarity to areA and dnr1, was disrupted [77]. Neither of these mutants have been studied in a virulence model. Virulence studies of these and other factors identified, for example in screens or through bioinformatics approaches, will be essential to determining the contribution of each factor to disease.

4. The Role of the Immune System

Fungal virulence is the result of interplay between the infecting organism and the host. During dermatophyte infection, cell-mediated immunity is widely considered to be responsible for modulating dermatophyte disease [7, 8287] and fungal antigens activate T-suppressor and T-helper cells [56]. Differences specific to the host are thought to be important in determining the relative susceptibility of individuals, with factors such as age, gender, and genetics all likely to play a role [85, 87]. These clinical factors will not be reviewed here.

A recent review of host-dermatophyte interactions is available [83]. We will briefly describe these as they relate to dermatophyte virulence factors. The most numerous cells in the epidermis are keratinocytes, indicating that dermatophytes must primarily interact with these cells. Interestingly, keratinocytes seem to exhibit a differential response following exposure to different dermatophyte species. Tani et al. measured cytokine production by epidermal keratinocytes following coculture with Tm, Tt, and Tr [88]. Of these, Tm causes an acute inflammatory response, whereas Tt and Tr are anthropophiles that cause minimal inflammation. Although all three species induced Interleukin- (IL-) 8 secretion, coculture of keratinocytes with Tm resulted in higher levels of IL-8 production than coculture with Tt or Tr. Additionally, Tm but not Tt or Tr was able to induce secretion of TNFα. Similar results were found when cytokine secretion profiles of human keratinocytes were compared during dermatophyte infection with Ab, a zoophile and causes a severe inflammatory response, and Tt [89]. They found that both species caused an increase in expression of IL-8, which was confirmed by reverse transcriptase-polymerase chain reaction (RT-PCR). However, Ab also induced secretion of a broad spectrum of cytokines, whereas Tt did not. These studies support the hypothesis that different dermatophyte species induce different immune responses in the host, contributing to the relative severity of the infection.

Keratinocytes are not the only cells that will interact with the dermatophytes. Phagocytic cells are attracted to the site of infection (reviewed in [87]), and an ability of dermatophytes to survive those interactions would contribute to pathogenesis. Campos et al. determined that Tr conidia could germinate in a macrophage, resulting in macrophage death [90].

Certainly, it would be advantageous for anthropophiles to downregulate the immune response so as to facilitate chronic infection, and fungal factors that modulate the host immune response represent potential virulence factors. Indeed, mannan extracted from the cell wall of Tr inhibited lymphoproliferation of human mononuclear leukocytes in vitro [91]. Addition of filtrate solution from Tm or Tr was shown to induce secretion of IL-1α  and basic fibroblast growth factor in keratinocytes [85], with more IL-1α  being secreted in cells exposed to the Tm filtrate. This suggests that at least some of the putative virulence factors involved in modulating the immune response might be secreted by the fungi. It is likely that cell-associated as well as secreted factors contribute to the dermatophyte’s ability to exaggerate or suppress an inflammatory response.

Temporal expression of proteases has also been postulated to contribute to the relative intensity of the inflammatory response [84]. Recent data comparing secreted proteolytic and lipolytic enzymes in Tt and Te support this idea [92]. Tt and Te are adapted to different host species (humans and horses, resp.), and Tt causes a mild chronic disease whereas Te causes an inflammatory disease in humans. Of the 31 genes studied, each had ≥99.5% sequence identity between the two species; however, transcriptional analysis identified differences in expression during growth on keratin [92]. For example, of the subtilisin-like proteases examined, Sub6 and Sub7 had significantly higher expression in Tt compared to Te, whereas Sub1 and Sub5 had significantly higher expression in Te compared to Tt [92].

Arthroconidia are produced during some infections and might aid survival in the nail and transmission of the infection to a new host. Arthroconidia can be formed by a majority of Tr clinical isolates during growth on nail powder under specific laboratory conditions [93] and have decreased susceptibility to some antifungals compared to microconidia [94]. The precise contribution of arthroconidia to infection and the mechanisms by which arthroconidia interact with host cells remains an area of investigation.

Few studies have examined dermatophyte gene expression in response to human cells [12, 30], and those that have serve to highlight the fact that growth in the presence of keratin does not necessarily reflect conditions during infection. The precise mechanisms by which dermatophyte species interact with host cells at the molecular level remain unknown. There is a clear need to identify the dermatophyte factors involved in pathogenesis, and a logical starting point is to identify dermatophyte genes and proteins that are upregulated during interactions with epithelial cells. To this end, transcriptional and proteomic profiling of dermatophytes during infection of human epidermal tissue, in addition to a bioinformatic approach, may identify additional potential virulence factors. These studies must go further, though. It is imperative that we test the expression and role that these factors play during infection. Only then can we expand our list of true virulence factors of dermatophytes and use the knowledge to inform directions for therapy and preventative measures.

Acknowledgments

The autors thank Drs. C. Cuomo, D. Martinez, M. Henn, and the rest of the staff at the Broad Institute who have contributed to the sequencing and annotation of the dermatophyte genomes. They thank Drs. J. Heitman and W. Li (Duke U.) for sharing their unpublished data about Tr mating types. They thank Drs. B. Oliver and D. Vinh (Seattle BioMed) for reading the paper. The authors were supported in part by R21-AI081235 awarded to T. C. White.

References

  1. E. S. Smith, S. R. Feldman, A. B. Fleischer, B. Leshin, and A. McMichael, “Characteristics of office-based visits for skin cancer: dermatologists have more experience than other physicians in managing malignant and premalignant skin conditions,” Dermatologic Surgery, vol. 24, no. 9, pp. 981–985, 1998. View at Scopus
  2. L. A. Drake, S. M. Dinehart, E. R. Farmer et al., “Guidelines of care for superficial mycotic infections of the skin: tinea corporis, tinea cruris, tinea faciei, tinea manuum, and tinea pedis,” Journal of the American Academy of Dermatology, vol. 34, no. 2 I, pp. 282–286, 1996. View at Publisher · View at Google Scholar · View at Scopus
  3. S. A. Marques, A. M. Robles, A. M. Tortorano, M. A. Tuculet, R. Negroni, and R. P. Mendes, “Mycoses associated with AIDS in the third world,” Medical Mycology, vol. 38, no. 1, pp. 269–279, 2000. View at Scopus
  4. T. C. White, B. G. Oliver, Y. Graser, and M. R. Henn, “Generating and testing molecular hypotheses in the dermatophytes,” Eukaryotic Cell, vol. 7, no. 8, pp. 1238–1245, 2008. View at Publisher · View at Google Scholar · View at Scopus
  5. G. E. J. Rodwell, C. L. Bayles, L. Towersey, and R. Aly, “The prevalence of dermatophyte infection in patients infected with human immunodeficiency virus,” International Journal of Dermatology, vol. 47, no. 4, pp. 339–343, 2008. View at Publisher · View at Google Scholar · View at Scopus
  6. A. K. Gupta and E. A. Cooper, “Update in antifungal therapy of dermatophytosis,” Mycopathologia, vol. 166, no. 5-6, pp. 353–367, 2008. View at Publisher · View at Google Scholar · View at Scopus
  7. I. Weitzman and R. C. Summerbell, “The dermatophytes,” Clinical Microbiology Reviews, vol. 8, no. 2, pp. 240–259, 1995. View at Scopus
  8. The Broad Institute, “Dermatophyte comparative database,” 2011, http://www.broadinstitute.org/annotation/genome/dermatophyte_comparative/MultiHome.html.
  9. S. M. Abdel-Rahman, N. Farrand, E. Schuenemann et al., “The prevalence of infections with Trichophyton tonsurans in schoolchildren: the CAPITIS study,” Pediatrics, vol. 125, no. 5, pp. 966–973, 2010. View at Publisher · View at Google Scholar · View at Scopus
  10. R. Sharma, S. De Hoog, W. Presber, and Y. Gräser, “A virulent genotype of Microsporum canis is responsible for the majority of human infections,” Journal of Medical Microbiology, vol. 56, no. 10, pp. 1377–1385, 2007. View at Publisher · View at Google Scholar · View at Scopus
  11. R. R. Achterman, A. R. Smith, B. G. Oliver, and T. C. White, “Sequenced dermatophyte strains: growth rate, conidiation, drug susceptibilities, and virulence in an invertebrate model,” Fungal Genetics and Biology, vol. 48, no. 3, pp. 335–341, 2011. View at Publisher · View at Google Scholar · View at Scopus
  12. A. Burmester, E. Shelest, G. Glockner et al., “Comparative and functional genomics provide insights into the pathogenicity of dermatophytic fungi,” Genome Biology, vol. 12, no. 1, article R7, 2011. View at Publisher · View at Google Scholar
  13. Y. Wu, J. Yang, F. Yang et al., “Recent dermatophyte divergence revealed by comparative and phylogenetic analysis of mitochondrial genomes,” BMC Genomics, vol. 10, article no. 238, 2009. View at Publisher · View at Google Scholar · View at Scopus
  14. B. I. Cantarel, P. M. Coutinho, C. Rancurel, T. Bernard, V. Lombard, and B. Henrissat, “The carbohydrate-active enZymes database (CAZy): an expert resource for glycogenomics,” Nucleic Acids Research, vol. 37, no. 1, pp. D233–D238, 2009. View at Publisher · View at Google Scholar · View at Scopus
  15. “Carbohydrate active enzymes database,” 2011, http://www.cazy.org.
  16. J. Heitman, “Evolution of eukaryotic microbial pathogens via covert sexual reproduction,” Cell host & Microbe, vol. 8, no. 1, pp. 86–99, 2010. View at Scopus
  17. J. Heitman, “Microbial pathogens in the fungal kingdom,” Fungal Biology Reviews, vol. 25, no. 1, pp. 48–60, 2011. View at Publisher · View at Google Scholar
  18. J. Heitman and W. Li, Duke University, personal communication, 2011.
  19. W. Li, B. Metin, T. C. White, and J. Heitman, “Organization and evolutionary trajectory of the mating type (MAT) locus in dermatophyte and dimorphic fungal pathogens,” Eukaryotic Cell, vol. 9, no. 1, pp. 46–58, 2010. View at Publisher · View at Google Scholar · View at Scopus
  20. K. Anzawa, M. Kawasaki, T. Mochizuki, and H. Ishizaki, “Successful mating of Trichophyton rubrum with Arthroderma simii,” Medical Mycology, vol. 48, no. 4, pp. 629–634, 2010. View at Publisher · View at Google Scholar · View at Scopus
  21. S. Vermout, J. Tabart, A. Baldo, M. Monod, B. Losson, and B. Mignon, “RNA silencing in the dermatophyte Microsporum canis,” FEMS Microbiology Letters, vol. 275, no. 1, pp. 38–45, 2007. View at Publisher · View at Google Scholar · View at Scopus
  22. S. Youngchim, S. Pornsuwan, J. D. Nosanchuk, W. Dankai, and N. Vanittanakom, “Melanogenesis in dermatophyte species in vitro and during infection,” Microbiology, vol. 157, pp. 2348–2356, 2011.
  23. A. K. Gupta, I. Ahmad, I. Borst, and R. C. Summerbell, “Detection of xanthomegnin in epidermal materials infected with Trichophyton rubrum,” Journal of Investigative Dermatology, vol. 115, no. 5, pp. 901–905, 2000. View at Publisher · View at Google Scholar · View at Scopus
  24. TrEd, “T. rubrum expression database (TrED),” 2011.
  25. J. Yang, L. Chen, L. Wang, W. Zhang, T. Liu, and Q. Jin, “TrED: the Trichophyton rubrum expression database,” BMC Genomics, vol. 8, article no. 250, 2007. View at Publisher · View at Google Scholar · View at Scopus
  26. F. C. Viani, J. I. Dos Santos, C. R. Paula, C. E. Larson, and W. Gambale, “Production of extracellular enzymes by Microsporum canis and their role in its virulence,” Medical Mycology, vol. 39, no. 5, pp. 463–468, 2001. View at Scopus
  27. M. Monod, “Secreted proteases from dermatophytes,” Mycopathologia, vol. 166, no. 5-6, pp. 285–294, 2008. View at Publisher · View at Google Scholar · View at Scopus
  28. F. C.A. Maranhão, F. G. Paião, and N. M. Martinez-Rossi, “Isolation of transcripts over-expressed in human pathogen Trichophyton rubrum during growth in keratin,” Microbial Pathogenesis, vol. 43, no. 4, pp. 166–172, 2007. View at Publisher · View at Google Scholar
  29. L. C. Baeza, A. M. Bailão, C. L. Borges, M. Pereira, C. M. D. A. Soares, and M. J. S. Mendes Giannini, “cDNA representational difference analysis used in the identification of genes expressed by Trichophyton rubrum during contact with keratin,” Microbes and Infection, vol. 9, no. 12-13, pp. 1415–1421, 2007. View at Publisher · View at Google Scholar · View at Scopus
  30. G. Kaufman, I. Berdicevsky, J. A. Woodfolk, and B. A. Horwitz, “Markers for host-induced gene expression in Trichophyton dermatophytosis,” Infection and Immunity, vol. 73, no. 10, pp. 6584–6590, 2005. View at Publisher · View at Google Scholar · View at Scopus
  31. C. Zaugg, M. Monod, J. Weber et al., “Gene expression profiling in the human pathogenic dermatophyte Trichophyton rubrum during growth on proteins,” Eukaryotic Cell, vol. 8, no. 2, pp. 241–250, 2009. View at Publisher · View at Google Scholar · View at Scopus
  32. M. C. Lorenz and G. R. Fink, “Life and death in a macrophage: role of the glyoxylate cycle in virulence,” Eukaryotic Cell, vol. 1, no. 5, pp. 657–662, 2002. View at Publisher · View at Google Scholar · View at Scopus
  33. P. Staib, C. Zaugg, B. Mignon et al., “Differential gene expression in the pathogenic dermatophyte Arthroderma benhamiae in vitro versus during infection,” Microbiology, vol. 156, no. 3, pp. 884–895, 2010. View at Publisher · View at Google Scholar · View at Scopus
  34. N. Youssef, C. H. E. Wyborn, and G. Holt, “Antibiotic production by dermatophyte fungi,” Journal of General Microbiology, vol. 105, no. 1, pp. 105–111, 1978. View at Scopus
  35. H. M. Lappin-Scott, M. E. Rogers, and M. W. Adlard, “High-performance liquid chromatographic identification of beta-lactam antibiotics produced by dermatophytes,” Journal of Applied Bacteriology, vol. 59, no. 5, pp. 437–441, 1985. View at Scopus
  36. W. Leng, T. Liu, J. Wang, R. Li, and Q. Jin, “Expression dynamics of secreted protease genes in Trichophyton rubrum induced by key host's proteinaceous components,” Medical Mycology, vol. 47, no. 7, pp. 759–765, 2009. View at Publisher · View at Google Scholar · View at Scopus
  37. F. C. Maranhao, H. C. Silveira, A. Rossi, and N. M. Martinez-Rossi, “Isolation of transcripts overexpressed in the human pathogen Trichophyton rubrum grown in lipid as carbon source,” Canadian Journal of Microbiology, vol. 57, no. 4, pp. 333–338, 2011.
  38. N. T. Peres, P. R. Sanches, J. P. Falco et al., “Transcriptional profiling reveals the expression of novel genes in response to various stimuli in the human dermatophyte Trichophyton rubrum,” BMC Microbiology, vol. 10, article no. 39, 2010. View at Publisher · View at Google Scholar · View at Scopus
  39. H. C. S. Silveira, D. E. Gras, R. A. Cazzaniga, P. R. Sanches, A. Rossi, and N. M. Martinez-Rossi, “Transcriptional profiling reveals genes in the human pathogen Trichophyton rubrum that are expressed in response to pH signaling,” Microbial Pathogenesis, vol. 48, no. 2, pp. 91–96, 2010. View at Publisher · View at Google Scholar · View at Scopus
  40. Y. Diao, R. Zhao, X. Deng, W. Leng, J. Peng, and Q. Jin, “Transcriptional profiles of Trichophyton rubrum in response to itraconazole,” Medical Mycology, vol. 47, no. 3, pp. 237–247, 2009. View at Publisher · View at Google Scholar · View at Scopus
  41. W. Zhang, L. Yu, W. Leng et al., “cDNA microarray analysis of the expression profiles of Trichophyton rubrum in response to novel synthetic fatty acid synthase inhibitor PHS11A,” Fungal Genetics and Biology, vol. 44, no. 12, pp. 1252–1261, 2007. View at Publisher · View at Google Scholar · View at Scopus
  42. W. Zhang, L. Yu, J. Yang, L. Wang, J. Peng, and Q. Jin, “Transcriptional profiles of response to terbinafine in Trichophyton rubrum,” Applied Microbiology and Biotechnology, vol. 82, no. 6, pp. 1123–1130, 2009. View at Publisher · View at Google Scholar · View at Scopus
  43. L. Yu, W. Zhang, L. Wang et al., “Transcriptional profiles of the response to ketoconazole and amphotericin B in Trichophyton rubrum,” Antimicrobial Agents and Chemotherapy, vol. 51, no. 1, pp. 144–153, 2007. View at Publisher · View at Google Scholar · View at Scopus
  44. F. G. Paião, F. Segato, J. R. Cursino-Santos, N. T. A. Peres, and N. M. Martinez-Rossi, “Analysis of Trichophyton rubrum gene expression in response to cytotoxic drugs,” FEMS Microbiology Letters, vol. 271, no. 2, pp. 180–186, 2007. View at Publisher · View at Google Scholar · View at Scopus
  45. F. Segato, S. R. Nozawa, A. Rossi, and N. M. Martinez-Rossi, “Over-expression of genes coding for proline oxidase, riboflavin kinase, cytochrome c oxidase and an MFS transporter induced by acriflavin in Trichophyton rubrum,” Medical Mycology, vol. 46, no. 2, pp. 135–139, 2008. View at Publisher · View at Google Scholar · View at Scopus
  46. X. Xu, T. Liu, W. Leng et al., “Global gene expression profiles for the growth phases of Trichophyton rubrum,” Science China Life Sciences, vol. 54, no. 7, pp. 675–682, 2011. View at Publisher · View at Google Scholar
  47. W. Leng, T. Liu, R. Li et al., “Proteomic profile of dormant Trichophyton Rubrum conidia,” BMC Genomics, vol. 9, article 303, 2008. View at Publisher · View at Google Scholar · View at Scopus
  48. L. Yang, L. Wang, J. Peng et al., “Comparison between gene expression of conidia and germinating phase in Trichophyton rubrum,” Science in China. Series C, vol. 50, no. 3, pp. 377–384, 2007. View at Publisher · View at Google Scholar · View at Scopus
  49. T. Liu, Q. Zhang, L. Wang et al., “The use of global transcriptional analysis to reveal the biological and cellular events involved in distinct development phases of Trichophyton rubrum conidial germination,” BMC Genomics, vol. 8, article 100, 2007. View at Publisher · View at Google Scholar · View at Scopus
  50. J. H. Reinhardt, A. M. Allen, D. Gunnison, and W. A. Akers, “Experimental human Trichophyton mentagrophytes infections,” Journal of Investigative Dermatology, vol. 63, no. 5, pp. 419–422, 1974. View at Scopus
  51. J. H. Greenberg, R. D. King, S. Krebs, and R. Field, “A quantitative dermatophyte infection model in the guinea pig: a parallel to the quantitated human infection model,” Journal of Investigative Dermatology, vol. 67, no. 6, pp. 704–708, 1976. View at Scopus
  52. A. Baldo, A. Mathy, J. Tabart et al., “Secreted subtilisin Sub3 from Microsporum canis is required for adherence to but not for invasion of the epidermis,” British Journal of Dermatology, vol. 162, no. 5, pp. 990–997, 2010. View at Publisher · View at Google Scholar · View at Scopus
  53. M. Grumbt, V. Defaweux, B. Mignon et al., “Targeted gene deletion and in vivo analysis of putative virulence gene function in the pathogenic dermatophyte Arthroderma benhamiae,” Eukaryotic Cell, vol. 10, no. 6, pp. 842–853, 2011. View at Publisher · View at Google Scholar
  54. B. R. Mignon, T. Leclipteux, C. Focant, A. J. Nikkels, G. E. Piérard, and B. J. Losson, “Humoral and cellular immune response to a crude exo-antigen and purified keratinase of Microsporum canis in experimentally infected guinea pigs,” Medical Mycology, vol. 37, no. 2, pp. 123–129, 1999. View at Publisher · View at Google Scholar · View at Scopus
  55. R. J. Hay, R. A. Calderon, and M. J. Collins, “Experimental dermatophytosis: the clinical and histopathologic features of a mouse model using Trichophyton quinckeanum (mouse favus),” Journal of Investigative Dermatology, vol. 81, no. 3, pp. 270–274, 1983. View at Scopus
  56. R. A. Calderon, “Immunoregulation of dermatophytosis,” Critical Reviews in Microbiology, vol. 16, no. 5, pp. 339–368, 1989. View at Scopus
  57. M. S. Ferreira-Nozawa, H. C. S. Silveira, C. J. Ono, A. L. Fachin, A. Rossi, and N. M. Martinez-Rossi, “The pH signaling transcription factor PacC mediates the growth of Trichophyton rubrum on human nail in vitro,” Medical Mycology, vol. 44, no. 7, pp. 641–645, 2006. View at Publisher · View at Google Scholar · View at Scopus
  58. F. C.A. Maranhão, F. G. Paião, A. L. Fachin, and N. M. Martinez-Rossi, “Membrane transporter proteins are involved in Trichophyton rubrum pathogenesis,” Journal of Medical Microbiology, vol. 58, no. 2, pp. 163–168, 2009. View at Publisher · View at Google Scholar
  59. G. Cotter, S. Doyle, and K. Kavanagh, “Development of an insect model for the in vivo pathogenicity testing of yeasts,” FEMS Immunology and Medical Microbiology, vol. 27, no. 2, pp. 163–169, 2000. View at Publisher · View at Google Scholar · View at Scopus
  60. J. C. Jackson, L. A. Higgins, and X. Lin, “Conidiation color mutants of Aspergillus fumigatus are highly pathogenic to the heterologous insect host Galleria mellonella,” PLoS ONE, vol. 4, no. 1, Article ID e4224, 2009. View at Publisher · View at Google Scholar · View at Scopus
  61. E. Mylonakis, “Galleria mellonella and the study of fungal pathogenesis: making the case for another genetically tractable model host,” Mycopathologia, vol. 165, no. 1, pp. 1–3, 2008. View at Publisher · View at Google Scholar · View at Scopus
  62. E. Mylonakis, R. Moreno, J. B. El Khoury et al., “Galleria mellonella as a model system to study Cryptococcus neoformans pathogenesis,” Infection and Immunity, vol. 73, no. 7, pp. 3842–3850, 2005. View at Publisher · View at Google Scholar · View at Scopus
  63. E. P. Reeves, C. G. M. Messina, S. Doyle, and K. Kavanagh, “Correlation between gliotoxin production and virulence of Aspergillus fumigatus in Galleria mellonella,” Mycopathologia, vol. 158, no. 1, pp. 73–79, 2004. View at Publisher · View at Google Scholar · View at Scopus
  64. J. Renwick, P. Daly, E. P. Reeves, and K. Kavanagh, “Susceptibility of larvae of Galleria mellonella to infection by Aspergillus fumigatus is dependent upon stage of conidial germination,” Mycopathologia, vol. 161, no. 6, pp. 377–384, 2006. View at Publisher · View at Google Scholar · View at Scopus
  65. R. J. S. Leger, S. E. Screen, and B. Shams-Pirzadeh, “Lack of host specialization in Aspergillus flavus,” Applied and Environmental Microbiology, vol. 66, no. 1, pp. 320–324, 2000. View at Scopus
  66. K. Kavanagh and E. P. Reeves, “Exploiting the potential of insects for in vivo pathogenicity testing of microbial pathogens,” FEMS Microbiology Reviews, vol. 28, no. 1, pp. 101–112, 2004. View at Publisher · View at Google Scholar · View at Scopus
  67. L. Duek, G. Kaufman, Y. Ulman, and I. Berdicevsky, “The pathogenesis of dermatophyte infections in human skin sections,” Journal of Infection, vol. 48, no. 2, pp. 175–180, 2004. View at Publisher · View at Google Scholar · View at Scopus
  68. G. Kaufman, B. Horwitz, L. Duek, Y. Ullman, and I. Berdicevsky, “Infection stages of the dermatophyte pathogen Trichophyton: microscopic characterization and proteolytic enzymes,” Medical Mycology, vol. 45, no. 2, pp. 149–155, 2007. View at Publisher · View at Google Scholar · View at Scopus
  69. G. Kaufman, B. A. Horwitz, R. Hadar, Y. Ullmann, and I. Berdicevsky, “Green fluorescent protein (GFP) as a vital marker for pathogenic development of the dermatophyte Trichophyton mentagrophytes,” Microbiology, vol. 150, no. 8, pp. 2785–2790, 2004. View at Scopus
  70. C. Onyewu, E. Eads, W. A. Schell et al., “Targeting the calcineurin pathway enhances ergosterol biosynthesis inhibitors against Trichophyton mentagrophytes in vitro and in a human skin infection model,” Antimicrobial Agents and Chemotherapy, vol. 51, no. 10, pp. 3743–3746, 2007. View at Publisher · View at Google Scholar · View at Scopus
  71. T. G. M. Smijs, J. A. Bouwstra, H. J. Schuitmaker, M. Talebi, and S. Pavel, “A novel ex vivo skin model to study the susceptibility of the dermatophyte Trichophyton rubrum to photodynamic treatment in different growth phases,” Journal of Antimicrobial Chemotherapy, vol. 59, no. 3, pp. 433–440, 2007. View at Publisher · View at Google Scholar · View at Scopus
  72. J. Tabart, A. Baldo, S. Vermout et al., “Reconstructed interfollicular feline epidermis as a model for Microsporum canis dermatophytosis,” Journal of Medical Microbiology, vol. 56, no. 7, pp. 971–975, 2007. View at Publisher · View at Google Scholar · View at Scopus
  73. M. M. Alshahni, T. Yamada, K. Takatori, T. Sawada, and K. Makimura, “Insights into a nonhomologous integration pathway in the dermatophyte Trichophyton mentagrophytes: efficient targeted gene disruption by use of mutants lacking ligase IV,” Microbiology and Immunology, vol. 55, no. 1, pp. 34–43, 2011. View at Publisher · View at Google Scholar · View at Scopus
  74. M. Grumbt, M. Monod, and P. Staib, “Genetic advances in dermatophytes,” FEMS Microbiology Letters, vol. 320, no. 2, pp. 79–86, 2011. View at Publisher · View at Google Scholar
  75. T. Yamada, “Development of efficient tools for genetic manipulation of dermatophytes,” Nihon Ishinkin Gakkai Zasshi, vol. 51, no. 2, pp. 87–92, 2010. View at Publisher · View at Google Scholar
  76. T. Yamada, K. Makimura, T. Hisajima, Y. Ishihara, Y. Umeda, and S. Abe, “Enhanced gene replacements in Ku80 disruption mutants of the dermatophyte, Trichophyton mentagrophytes,” FEMS Microbiology Letters, vol. 298, no. 2, pp. 208–217, 2009. View at Publisher · View at Google Scholar · View at Scopus
  77. T. Yamada, K. Makimura, K. Satoh, Y. Umeda, Y. Ishihara, and S. Abe, “Agrobacterium tumefaciens-mediated transformation of the dermatophyte, Trichophyton mentagrophytes: an efficient tool for gene transfer,” Medical Mycology, vol. 47, no. 5, pp. 485–495, 2009. View at Publisher · View at Google Scholar · View at Scopus
  78. A. L. Fachin, M. S. Ferreira-Nozawa, W. Maccheroni, and N. M. Martinez-Rossi, “Role of the ABC transporter TruMDR2 in terbinafine, 4-nitroquinoline N-oxide and ethidium bromide susceptibility in Trichophyton rubrum,” Journal of Medical Microbiology, vol. 55, no. 8, pp. 1093–1099, 2006. View at Publisher · View at Google Scholar · View at Scopus
  79. B. Mignon, M. Swinnen, J. P. Bouchara et al., “Purification and characterization of a 315 kDa keratinolytic subtilisin-like serine protease from Microsporum canis and evidence of its secretion in naturally infected cats,” Medical Mycology, vol. 36, no. 6, pp. 395–404, 1998. View at Scopus
  80. B. R. Mignon, A. F. Nikkels, G. E. Piérard, and B. J. Losson, “The in vitro and in vivo production of a 31.5-kD keratinolytic subtilase from Microsporum canis and the clinical status in naturally infected cats,” Dermatology, vol. 196, no. 4, pp. 438–441, 1998. View at Publisher · View at Google Scholar · View at Scopus
  81. T. Yamada, K. Makimura, and S. Abe, “Isolation, characterization, and disruption of dnr1, the areA/nit-2 -like nitrogen regulatory gene of the zoophilic dermatophyte, Microsporum canis,” Medical Mycology, vol. 44, no. 3, pp. 243–252, 2006. View at Publisher · View at Google Scholar · View at Scopus
  82. S. R. Almeida, “Immunology of dermatophytosis,” Mycopathologia, vol. 166, no. 5-6, pp. 277–283, 2008. View at Publisher · View at Google Scholar · View at Scopus
  83. N. T. De Aguiar Peres, F. C. A. Maranhão, A. Rossi, and N. M. Martinez-Rossi, “Dermatophytes: host-pathogen interaction and antifungal resistance,” Anais Brasileiros de Dermatologia, vol. 85, no. 5, pp. 657–667, 2010. View at Scopus
  84. S. Vermout, J. Tabart, A. Baldo, A. Mathy, B. Losson, and B. Mignon, “Pathogenesis of dermatophytosis,” Mycopathologia, vol. 166, no. 5-6, pp. 267–275, 2008. View at Publisher · View at Google Scholar · View at Scopus
  85. H. Ogawa, R. C. Summerbell, K. V. Clemons et al., “Dermatophytes and host defence in cutaneous mycoses,” Medical Mycology, vol. 36, no. 1, Supplement 1, pp. 166–173, 1998. View at Scopus
  86. M. V. Dahl, “Suppression of immunity and inflammation by products produced by dermatophytes,” Journal of the American Academy of Dermatology, vol. 28, no. 5 I, pp. S19–S23, 1993. View at Scopus
  87. J. Brasch, “Current knowledge of host response in human tinea,” Mycoses, vol. 52, no. 4, pp. 304–312, 2009. View at Publisher · View at Google Scholar · View at Scopus
  88. K. Tani, M. Adachi, Y. Nakamura et al., “The effect of dermatophytes on cytokine production by human keratinocytes,” Archives of Dermatological Research, vol. 299, no. 8, pp. 381–387, 2007. View at Publisher · View at Google Scholar · View at Scopus
  89. Y. Shiraki, Y. Ishibashi, M. Hiruma, A. Nishikawa, and S. Ikeda, “Cytokine secretion profiles of human keratinocytes during Trichophyton tonsurans and Arthroderma benhamiae infections,” Journal of Medical Microbiology, vol. 55, no. 9, pp. 1175–1185, 2006. View at Publisher · View at Google Scholar · View at Scopus
  90. M. R. M. Campos, M. Russo, E. Gomes, and S. R. Almeida, “Stimulation, inhibition and death of macrophages infected with Trichophyton rubrum,” Microbes and Infection, vol. 8, no. 2, pp. 372–379, 2006. View at Publisher · View at Google Scholar · View at Scopus
  91. J. S. Blake, M. V. Dahl, M. J. Herron, and R. D. Nelson, “An immunoinhibitory cell wall glycoprotein (mannan) from Trichophyton rubrum,” Journal of Investigative Dermatology, vol. 96, no. 5, pp. 657–661, 1991. View at Scopus
  92. B. L. Preuett, E. Schuenemann, J. T. Brown, M. E. Kovac, S. K. Krishnan, and S. M. Abdel-Rahman, “Comparative analysis of secreted enzymes between the anthropophilic-zoophilic sister species Trichophyton tonsurans and Trichophyton equinum,” Fungal Biology, vol. 114, no. 5-6, pp. 429–437, 2010. View at Publisher · View at Google Scholar · View at Scopus
  93. S. A. Yazdanparast and R. C. Barton, “Arthroconidia production in Trichophyton rubrum and a new ex vivo model of onychomycosis,” Journal of Medical Microbiology, vol. 55, no. 11, pp. 1577–1581, 2006. View at Publisher · View at Google Scholar · View at Scopus
  94. L. M. Coelho, R. Aquino-Ferreira, C. M. L. Maffei, and N. M. Martinez-Rossi, “In vitro antifungal drug susceptibilities of dermatophytes microconidia and arthroconidia,” Journal of Antimicrobial Chemotherapy, vol. 62, no. 4, pp. 758–761, 2008. View at Publisher · View at Google Scholar · View at Scopus